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SURGICAL PREP RAZOR

K781437 Traditional
Decision Date
1978-12-05
Sponsor / Applicant
Warren J. Grosjean

Technical Specification

510(k) Submission ID K781437
Product Code LDQ
Medical Specialty / Panel General Hospital
Decision Date 1978-12-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SURGICAL PREP RAZOR received FDA 510(k) clearance under submission number K781437, sponsored by Warren J. Grosjean. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1978-12-05.

Classification & Regulation

This clearance is catalogued under FDA product code LDQ , within the General Hospital review panel as a device.